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CHEMISTRY OF PACLITAXEL( NATURAL CHEMISTRY).pptx

  1. GURU NANAK INSTITUTE OF PHARMACEUTICAL SCIENCE AND TECHNOLOGY (An Autonomous Institute) TOPIC :CHEMISTRY AND ANTI CANCER ACTIVITY OF PACLITAXEL. NAME OF THE STUDENT: MD JAVED ROLL NO:186112201008 ACADEMIC SESSION: 2022-2024 PAPER NAME: Chemistry of Natural Product. PAPER CODE:MPT 1034 Affiliated to MaulanaAbul KalamAzad University of Technology
  2. CONTENT 1. Introduction 2. Structure 3. Derivatives of paclitaxel 4. Mechanism 5. Chemistry of paclitaxel 6. Summary 7. Reference
  3. INTRODUCTION • It is isolated from the bark of Taxus brevifolia. • It was discovered by Monroe E.Wall and Mansukh wani. • Paclitaxel belongs to class of chemotherapy drug called plant alkaloid. • It is used as an anticancer drug. • It interferes with the growth of microtubules.(1) • BRAND NAMES: Abraxane,Taxone • GENERIC NAMES: Paclitaxel • CHEMICAL FORMULA: C47H51NO14
  4. STRUCTURE
  5. DERIVATES OF PACLITAXEL DOCETAXEL- Treatment of breast cancer. ORTATAXEL- Treatment of lung cancer, lymphoma and kidney cancer.(2) LAROTAXEL- Treatment of Pancreatic cancer. TESETAXEL- Orally administered Taxane. DOCETAXEL ORTATAXEL TESETAXEL
  6. MECHANISM OF ACTION  Target microtubule.  Microtubule are required for maintenance of cell structure, motility and cytoplasmic movement within cell.  In simple words Paclitaxel stops cancer cells from separating into 2 new cell.  This blocks the growth of cancer.(2)
  7. CHEMISTRY OF PACLITAXEL • The nomenclature of paclitaxel is structured on 17 atom skeleton tetracyclic. • There are total 11 stereo center.(3)
  8. SUMMARY • Paclitaxel is most widely used antineoplastic agent with broad activity in several cancer. • In 1992 paclitaxel was approved by US-FDA for treatment of ovarian cancer. • Paclitaxel alone s used for treatment of metastatic ovarian cancer. • The abundance of paclitaxel is low in original bark of yew tree so the prices are high. • Side effects are not so severe like vomiting, loss of appetite, pain in joints and legs.
  9. REFERENCE 1.D Sriram, P Yogeeswari, “Medicinal Chemistry”, pp 2-4, 2018. 2. Fu Y, Li S, Zu Y, Yang G, Yang Z, Luo M, Jiang S, Wink M, Efferth T. Medicinal chemistry of paclitaxel and its analogues. Curr Med Chem. 2009;16(30):3966-85. doi: 10.2174/092986709789352277. PMID: 19747129. 3. N J Fauzee, “Taxanes: promising anticancer drugs”, Asian Pac J Cancer prev. Vol 12(4), pp 837-851, 2011.
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